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WO2021187510A1 - Procédé de réticulation de protéines - Google Patents

Procédé de réticulation de protéines Download PDF

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Publication number
WO2021187510A1
WO2021187510A1 PCT/JP2021/010764 JP2021010764W WO2021187510A1 WO 2021187510 A1 WO2021187510 A1 WO 2021187510A1 JP 2021010764 W JP2021010764 W JP 2021010764W WO 2021187510 A1 WO2021187510 A1 WO 2021187510A1
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Prior art keywords
protein
enzyme
laccase
cross
linking
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Ceased
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PCT/JP2021/010764
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English (en)
Japanese (ja)
Inventor
杏匠 酒井
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Amano Enzyme Inc
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Amano Enzyme Inc
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Priority to EP21771002.9A priority Critical patent/EP4122327A4/fr
Priority to JP2022508399A priority patent/JPWO2021187510A1/ja
Priority to CA3171481A priority patent/CA3171481A1/fr
Priority to CN202180020879.4A priority patent/CN115298320A/zh
Priority to BR112022017511A priority patent/BR112022017511A2/pt
Priority to US17/906,498 priority patent/US20230114377A1/en
Publication of WO2021187510A1 publication Critical patent/WO2021187510A1/fr
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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    • A—HUMAN NECESSITIES
    • A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23C—DAIRY PRODUCTS, e.g. MILK, BUTTER OR CHEESE; MILK OR CHEESE SUBSTITUTES; MAKING OR TREATMENT THEREOF
    • A23C19/00—Cheese; Cheese preparations; Making thereof
    • A23C19/02—Making cheese curd
    • A23C19/032—Making cheese curd characterised by the use of specific microorganisms, or enzymes of microbial origin
    • A23C19/0328—Enzymes other than milk clotting enzymes, e.g. lipase, beta-galactosidase
    • A—HUMAN NECESSITIES
    • A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23C—DAIRY PRODUCTS, e.g. MILK, BUTTER OR CHEESE; MILK OR CHEESE SUBSTITUTES; MAKING OR TREATMENT THEREOF
    • A23C20/00—Cheese substitutes
    • A—HUMAN NECESSITIES
    • A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23C—DAIRY PRODUCTS, e.g. MILK, BUTTER OR CHEESE; MILK OR CHEESE SUBSTITUTES; MAKING OR TREATMENT THEREOF
    • A23C9/00—Milk preparations; Milk powder or milk powder preparations
    • A23C9/12—Fermented milk preparations; Treatment using microorganisms or enzymes
    • A23C9/1203—Addition of, or treatment with, enzymes or microorganisms other than lactobacteriaceae
    • A23C9/1209—Proteolytic or milk coagulating enzymes, e.g. trypsine
    • A—HUMAN NECESSITIES
    • A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23C—DAIRY PRODUCTS, e.g. MILK, BUTTER OR CHEESE; MILK OR CHEESE SUBSTITUTES; MAKING OR TREATMENT THEREOF
    • A23C9/00—Milk preparations; Milk powder or milk powder preparations
    • A23C9/12—Fermented milk preparations; Treatment using microorganisms or enzymes
    • A23C9/1203—Addition of, or treatment with, enzymes or microorganisms other than lactobacteriaceae
    • A23C9/1213—Oxidation or reduction enzymes, e.g. peroxidase, catalase, dehydrogenase
    • A—HUMAN NECESSITIES
    • A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23C—DAIRY PRODUCTS, e.g. MILK, BUTTER OR CHEESE; MILK OR CHEESE SUBSTITUTES; MAKING OR TREATMENT THEREOF
    • A23C9/00—Milk preparations; Milk powder or milk powder preparations
    • A23C9/12—Fermented milk preparations; Treatment using microorganisms or enzymes
    • A23C9/1203—Addition of, or treatment with, enzymes or microorganisms other than lactobacteriaceae
    • A23C9/1216—Other enzymes
    • A—HUMAN NECESSITIES
    • A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23J—PROTEIN COMPOSITIONS FOR FOODSTUFFS; WORKING-UP PROTEINS FOR FOODSTUFFS; PHOSPHATIDE COMPOSITIONS FOR FOODSTUFFS
    • A23J3/00—Working-up of proteins for foodstuffs
    • A23J3/30—Working-up of proteins for foodstuffs by hydrolysis
    • A23J3/32—Working-up of proteins for foodstuffs by hydrolysis using chemical agents
    • A23J3/34—Working-up of proteins for foodstuffs by hydrolysis using chemical agents using enzymes
    • A—HUMAN NECESSITIES
    • A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23J—PROTEIN COMPOSITIONS FOR FOODSTUFFS; WORKING-UP PROTEINS FOR FOODSTUFFS; PHOSPHATIDE COMPOSITIONS FOR FOODSTUFFS
    • A23J3/00—Working-up of proteins for foodstuffs
    • A23J3/30—Working-up of proteins for foodstuffs by hydrolysis
    • A23J3/32—Working-up of proteins for foodstuffs by hydrolysis using chemical agents
    • A23J3/34—Working-up of proteins for foodstuffs by hydrolysis using chemical agents using enzymes
    • A23J3/341—Working-up of proteins for foodstuffs by hydrolysis using chemical agents using enzymes of animal proteins
    • A—HUMAN NECESSITIES
    • A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23J—PROTEIN COMPOSITIONS FOR FOODSTUFFS; WORKING-UP PROTEINS FOR FOODSTUFFS; PHOSPHATIDE COMPOSITIONS FOR FOODSTUFFS
    • A23J3/00—Working-up of proteins for foodstuffs
    • A23J3/30—Working-up of proteins for foodstuffs by hydrolysis
    • A23J3/32—Working-up of proteins for foodstuffs by hydrolysis using chemical agents
    • A23J3/34—Working-up of proteins for foodstuffs by hydrolysis using chemical agents using enzymes
    • A23J3/341—Working-up of proteins for foodstuffs by hydrolysis using chemical agents using enzymes of animal proteins
    • A23J3/343—Working-up of proteins for foodstuffs by hydrolysis using chemical agents using enzymes of animal proteins of dairy proteins
    • A23J3/344—Working-up of proteins for foodstuffs by hydrolysis using chemical agents using enzymes of animal proteins of dairy proteins of casein
    • A—HUMAN NECESSITIES
    • A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23J—PROTEIN COMPOSITIONS FOR FOODSTUFFS; WORKING-UP PROTEINS FOR FOODSTUFFS; PHOSPHATIDE COMPOSITIONS FOR FOODSTUFFS
    • A23J3/00—Working-up of proteins for foodstuffs
    • A23J3/30—Working-up of proteins for foodstuffs by hydrolysis
    • A23J3/32—Working-up of proteins for foodstuffs by hydrolysis using chemical agents
    • A23J3/34—Working-up of proteins for foodstuffs by hydrolysis using chemical agents using enzymes
    • A23J3/346—Working-up of proteins for foodstuffs by hydrolysis using chemical agents using enzymes of vegetable proteins
    • A—HUMAN NECESSITIES
    • A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23L—FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES, NOT OTHERWISE PROVIDED FOR; PREPARATION OR TREATMENT THEREOF
    • A23L29/00—Foods or foodstuffs containing additives; Preparation or treatment thereof
    • A23L29/06—Enzymes
    • A—HUMAN NECESSITIES
    • A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23L—FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES, NOT OTHERWISE PROVIDED FOR; PREPARATION OR TREATMENT THEREOF
    • A23L33/00—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
    • A23L33/10—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
    • A23L33/17—Amino acids, peptides or proteins
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
    • C12N9/0004—Oxidoreductases (1.)
    • C12N9/001—Oxidoreductases (1.) acting on the CH-CH group of donors (1.3)
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
    • C12N9/0004—Oxidoreductases (1.)
    • C12N9/0055—Oxidoreductases (1.) acting on diphenols and related substances as donors (1.10)
    • C12N9/0057—Oxidoreductases (1.) acting on diphenols and related substances as donors (1.10) with oxygen as acceptor (1.10.3)
    • C12N9/0061—Laccase (1.10.3.2)
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
    • C12N9/14—Hydrolases (3)
    • C12N9/78—Hydrolases (3) acting on carbon to nitrogen bonds other than peptide bonds (3.5)
    • C12N9/80—Hydrolases (3) acting on carbon to nitrogen bonds other than peptide bonds (3.5) acting on amide bonds in linear amides (3.5.1)
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12Y—ENZYMES
    • C12Y103/00—Oxidoreductases acting on the CH-CH group of donors (1.3)
    • C12Y103/03—Oxidoreductases acting on the CH-CH group of donors (1.3) with oxygen as acceptor (1.3.3)
    • C12Y103/03005—Bilirubin oxidase (1.3.3.5)
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12Y—ENZYMES
    • C12Y110/00—Oxidoreductases acting on diphenols and related substances as donors (1.10)
    • C12Y110/03—Oxidoreductases acting on diphenols and related substances as donors (1.10) with an oxygen as acceptor (1.10.3)
    • C12Y110/03002—Laccase (1.10.3.2)
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12Y—ENZYMES
    • C12Y305/00—Hydrolases acting on carbon-nitrogen bonds, other than peptide bonds (3.5)
    • C12Y305/01—Hydrolases acting on carbon-nitrogen bonds, other than peptide bonds (3.5) in linear amides (3.5.1)
    • C12Y305/01044—Protein-glutamine glutaminase (3.5.1.44)
    • A—HUMAN NECESSITIES
    • A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
    • A23V2200/00—Function of food ingredients
    • A23V2200/20—Ingredients acting on or related to the structure
    • A23V2200/21—Binding agent
    • A—HUMAN NECESSITIES
    • A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
    • A23V2200/00—Function of food ingredients
    • A23V2200/20—Ingredients acting on or related to the structure
    • A23V2200/228—Gelling agent
    • A—HUMAN NECESSITIES
    • A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
    • A23V2200/00—Function of food ingredients
    • A23V2200/20—Ingredients acting on or related to the structure
    • A23V2200/242—Thickening agent
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P21/00—Preparation of peptides or proteins

Definitions

  • the present invention relates to a novel method for cross-linking a protein using an enzyme. More specifically, the present invention relates to a method for cross-linking a protein using a combination of an oxidoreductase and a protein deamidating enzyme.
  • transglutaminase lysyl oxidase, protein disulfide isomerase, protein disulfide reductase, sulfhydryl oxidase, lipoxygenase, polyphenol oxidase (tyrosinase), peroxidase and the like are known as enzymes having a possibility of polymerizing a protein by a cross-linking reaction.
  • enzymes having a possibility of polymerizing a protein by a cross-linking reaction.
  • transglutaminase is well known as a protein cross-linking method using it. It is well known that it is widely used mainly in the food processing field due to the discovery of an inexpensive transglutaminase derived from a microorganism and which does not require the presence of calcium in the reaction (Patent Document 1, Non-Patent). See Reference 2).
  • transglutaminase forms a bridging structure within or between protein molecules as a result of the acyl transfer reaction that occurs between the ⁇ -carboxyl group of the glutamine residue in the protein and the ⁇ -amino group of the lysine residue. Since it is an enzyme, some proteins are difficult to serve as substrates due to lack of glutamine residue or lysine residue depending on the type of protein. For example, albumin proteins could not be substrates for transglutaminase in their native state.
  • a protein cross-linking method characterized by allowing an oxidoreductase and a protein deamidating enzyme to act on a protein.
  • the protein improver according to [7], wherein the redox enzyme is multi-copper oxidase.
  • the protein improver according to [8], wherein the multi-copper oxidase is laccase and / or bilirubin oxidase.
  • the protein improver according to [8], wherein the multi-copper oxidase is laccase.
  • the protein improving agent according to any one of [7] to [10], wherein the protein deamidating enzyme is an enzyme that acts on a glutamine residue in a protein.
  • the protein improver according to [11], wherein the protein deamidating enzyme is protein glutaminase.
  • a method for producing a crosslinked protein which comprises the following steps: (1) Step of treating protein with protein deamidating enzyme, (2) Protein A step of treating a deamidated protein with an oxidoreductase.
  • a method for producing a crosslinked protein which comprises the following steps: (1) Step of preparing a protein treated with a protein deamidating enzyme, (2) A step of treating the prepared protein with an oxidoreductase.
  • a method for producing a crosslinked protein which comprises a step of simultaneously treating a protein with an oxidoreductase and a protein deamidating enzyme.
  • a method for producing a food or pharmaceutical product which comprises the following steps: (1) A step of preparing a food raw material or a pharmaceutical raw material containing a protein, which has been treated with a protein deamidating enzyme. (2) A step of treating the prepared food raw material or pharmaceutical raw material with an oxidoreductase. [17] A method for producing a food or pharmaceutical product, which comprises a step of simultaneously treating a food material or a pharmaceutical material containing a protein with an oxidoreductase and a protein deamidating enzyme.
  • the cross-linking method of the present invention is characterized by allowing an oxidoreductase and a protein deamidating enzyme to act on a protein.
  • the oxidoreductase referred to in the present invention is not particularly limited as long as it is an enzyme that crosslinks a protein by a redox reaction, and examples thereof include the following. (1) An enzyme that cross-links a protein by oxidizing the ⁇ -amino group of lysine in the protein to generate a highly reactive aldehyde and forming a Schiff base with the amino group of another protein molecule (for example, lysyl oxidase).
  • An enzyme that cross-links a protein by oxidizing the sulfhydryl group of cysteine in the protein and forming a disulfhydryl bond with another protein molecule for example, sulfhydryl oxidase.
  • Crosslinking enzymes eg, multi-copper oxidases such as laccase
  • An enzyme eg, peroxidase that catalyzes the same reaction as (4) but requires hydrogen peroxide as an oxygen donor in the oxidation reaction.
  • multi-copper oxidase is a group of enzymes that contain a plurality of copper atoms in the molecule and oxidize polyphenols, methoxyphenols, diamines, birylbin, ascorbic acid, etc. with molecular oxygen.
  • the number of copper atoms contained is usually 2 to 8 known so far, but this number is particularly limited because it varies depending on the state of the enzyme preparation at the time of analysis and the analysis method. It's not a thing.
  • Examples of enzymes classified into multi-copper oxidase include laccase, bilirubin oxidase, ascorbic acid oxidase, and celluloplasmin.
  • Laccase [EC1.10.3.2] is a type of multi-copper protein with low substrate specificity that also acts on O-quinol, p-quinol or often aminophenols and phenylenediamines. It is an enzyme that has. The resulting semiquinone further reacts enzymatically or non-enzymatically.
  • laccases examples include those derived from plants such as lacquer and microorganisms such as bacteria and fungi (Fungi), and examples of laccases derived from microorganisms include Aspergillus, Neurospora, Podospora, Botrytis, Collybia, Fomes, Examples include enzymes from the genus Lentinus, Pleurotus, Pycnoporus, Pyricularia, Trametes, Rhizoctonia, Rigidoporus, Coprinus, Psatyrella, Myceliophtera, Schtalidium, Polyporus, Phlebia, Coriolus.
  • Bilirubin oxidase (EC1.3.3.5) is a type of multi-copper protein and is an enzyme that mainly acts on bilirubin. Examples of such bilirubin oxidase include enzymes derived from the genus Penicillium, Myrothecium, and Trachyderma. Be done.
  • Ascorbic acid oxidase (EC1.10.3.3) is a type of multi-copper protein, an enzyme that mainly acts on L-ascorbic acid, such as plants such as cucumber, pumpkin, and zucchini, and bacteria and fungi (Fungi). Some are derived from microorganisms.
  • Celluloplasmin (EC1.16.3.1) is a type of multi-copper protein, which is a multifunctional protein that maintains copper homeostasis in living organisms, has ferrooxidase activity, and amine oxidase activity, and is found in the serum of animals and birds. exist.
  • the protein deamidating enzyme as used in the present invention refers to an enzyme that catalyzes the reaction of liberating ammonia from a protein, and specifically, an enzyme that converts a glutamine residue in a protein into a glutamate residue (that is, protein glutaminase). Examples thereof include an enzyme that converts an asparagine residue into an aspartic acid residue (that is, a protein asparaginase), and a protein deimino enzyme that converts an arginine residue in a protein into a citrulin residue.
  • Examples of enzymes that deamidate glutamine residues in proteins include protein glutaminase derived from Chryseobacterium proteolyticum (EurJBiochem, 268 (5), 1410, 2001, Protein-glutaminaseFromChryseobacteriumProteolyticum, anEnzymeThatDeamidatesGlutaminylResiduesinProteins.Purination, AnEnzymeThatDeamidatesGlutaminylResiduesinProteins.
  • the deamidated protein has amphipathic properties and becomes an ideal surfactant, and the emulsifying power, emulsifying stability, foaming property, and foam stability of the protein are greatly improved.
  • deamidation of a protein results in an improvement in various functional properties of the protein, dramatically increasing its use (eg MolecularApproachestoImprovingFoodQualityandSafety, D.ChatnagarandT.E.Cleveland, eds., VanNostrandReinhold, New York). , 1992, p.37).
  • the arginine residue in the protein is deiminated, the hydrophobicity of the protein is increased and the higher-order structure of the protein is changed.
  • the present inventor newly discovered "a phenomenon in which a protein cross-linking reaction by an oxidative-reducing enzyme is promoted by the action of a protein deamidase" (see Examples described later).
  • a protein deamidase As a result of the unfolding of the protein and the change of the higher-order structure due to the action of the protein deamidating enzyme, the amino acid residues that are the targets of oxidative reduction enzymes such as cysteine and lysine, including tyrosine buried inside the protein molecule, are released. It can be explained that the exposure to the molecular surface of the protein made it more susceptible to the action of oxidative reductase.
  • the types and origins of the redox enzymes and protein deamidating enzymes that can be used in the present invention are not particularly limited.
  • the origin for example, it is derived from an animal, a plant, or a microorganism.
  • the enzyme may be accumulated inside or outside the microorganism.
  • it may be an enzyme protein modified by a protein engineering method.
  • oxidoreductase for example, multi-copper oxidase
  • protein deamidating enzyme for example, protein glutaminase
  • an enzyme preparation may be used as the oxidoreductase and the protein deamidating enzyme, and in that case, various salts, sugars, proteins, lipids, surfactants and the like are added as enzyme stabilizers to the enzyme preparation. May be.
  • the cross-linking method of the present invention can be applied to various proteins for which cross-linking is desired.
  • proteins for which cross-linking is desired.
  • the origin, properties, etc. of the protein that is the substrate for the redox enzyme and protein deamidating enzyme For example, in the case of vegetable proteins, legume-derived proteins such as soybeans, greenpeas, lentils, chickpeas, and blackbeans, wheat, barley, and swallow (Oat). ), Grain-derived proteins such as rice, nut-derived proteins such as almonds and peanuts, and seed-derived proteins such as cannabis seeds (Hemp), chia seeds (Chia), Chia (Quinoa), and Amaranthus. Take as an example.
  • Insect proteins such as crickets, yeast, filamentous fungi, fungal-derived proteins called mushroom mycoproteins, and algae-derived proteins such as spirulina can also be used.
  • animal proteins include casein, milk proteins such as ⁇ -lactoglobulin, egg proteins such as ovalbumin, meat proteins such as myosin and actin, blood proteins such as serum albumin, and tendon proteins such as gelatin and collagen.
  • a chemically partially decomposed protein such as an acid or an alkali
  • an enzymatic partially decomposed protein such as a protease, a chemically modified protein using various reagents, a synthetic peptide or the like can also be used as a substrate protein.
  • the above-mentioned substrate proteins are subjected to the reaction in a state of being contained in a fluid composition such as a solution, slurry or paste, but the concentration of the substrate protein in the fluid composition is not particularly limited. Instead, the concentration of the desired protein crosslinked product may be determined according to the desired properties and conditions. Generally, a solution or precipitate having increased viscosity can be obtained at a low concentration, and a gel-like substance can be obtained at a high concentration, but a gelled product can be sufficiently obtained when the substrate protein concentration is 1% by weight or more.
  • the fluid composition containing a substrate protein is not limited to a fluid composition in the form of an aqueous solution of a protein, an aqueous dispersion, or an aqueous dispersion paste, and these are fluid compositions in the form of an emulsion with fats and oils. May be subjected to the reaction, and salts, sugars, proteins, fragrances, moisturizers, colorants and the like may be added to the fluid composition containing the substrate protein, if necessary.
  • the amount of enzyme used, reaction time, temperature, pH of the reaction solution, etc. are not particularly limited. Usually, the amount of enzyme is 1 to 1000000 U, preferably 10 to 500,000 U, more preferably 100 to 200,000 U for oxidoreductase, and 0.01 to 100,000 U, preferably 0.1 to 50000 U, more preferably for protein deamidating enzyme with respect to 1 g of protein. It is 1 to 10000U.
  • the reaction temperature is 5 to 80 ° C, preferably 20 to 60 ° C.
  • the pH of the reaction solution is 2-10, preferably 4-8.
  • the reaction time is 10 seconds to 48 hours, preferably 10 minutes to 24 hours.
  • reaction conditions Under the above reaction conditions, a crosslinked product in which the protein is polymerized or a gel-like product of a fluid composition can be obtained.
  • reaction conditions are appropriately selected according to the physical characteristics and water content of the target protein crosslinked product or gel-like product of the fluid composition. The optimum reaction conditions may be determined through preliminary experiments.
  • multi-copper oxidase When multi-copper oxidase is used as the oxidative reduction enzyme, various polyphenols such as Hydroquinone, Catechol, Guaiacol, Ferulic acid, Vanillic acid, etc. are used as mediators to promote the reaction.
  • p-Coumaric acid, Syringaldehyde, p-Phenylenediamine and the like may be added.
  • the substrate protein is treated with a protein cross-linking enzyme, that is, an oxidoreductase and a protein deamidating enzyme.
  • a protein cross-linking enzyme that is, an oxidoreductase and a protein deamidating enzyme.
  • the order in which the enzymes are allowed to act is not particularly limited, but treatment with both enzymes at the same time, or treatment with protein deamide enzyme and then treatment with oxidoreductase. It is preferable to do so. Simultaneous processing is more preferable for the purpose of improving work efficiency.
  • a step of inactivating the protein deamidating enzyme after the treatment with the protein deamidating enzyme may be added.
  • the amount of protein deamidation can be adjusted by adding a deactivation step.
  • crosslinked protein or food or pharmaceutical product containing the crosslinked protein can be produced.
  • One aspect of the method for producing a crosslinked protein includes the following steps (1) and (2).
  • a step of inactivating the protein deamidating enzyme may be added after the step (1).
  • Step of treating protein with protein deamidating enzyme (2) Step of treating protein deamidated protein with oxidoreductase
  • steps (1) and (2) are performed.
  • Step of preparing protein treated with protein deamidating enzyme Step of treating prepared protein with oxidoreductase
  • the crosslinked protein is produced by the following step (i). (I) Step of simultaneously treating protein with redox enzyme and protein deamidating enzyme
  • one aspect of the method for producing foods and pharmaceuticals includes the following (1) and (2).
  • Step of preparing a food raw material or a pharmaceutical raw material containing a protein treated with a protein deamidating enzyme (2)
  • the food or pharmaceutical product is produced by the following step (i).
  • the present invention also provides a protein improver that can be used for protein cross-linking.
  • the protein improver of the present invention is typically utilized in the cross-linking method or production method of the present invention.
  • the protein improver of the present invention contains oxidoreductase and protein deamidating enzyme, which are enzymes for protein cross-linking, as active ingredients.
  • the protein improver of the present invention can be used as a protein cross-linking agent, preferably as a thickener for a fluid composition containing a protein, and more preferably as a gelling agent for a fluid composition containing a protein. Can be done. Since the details of the redox enzyme and the protein deamidating enzyme are as described in (1. Protein cross-linking method column), the description thereof will be omitted.
  • ⁇ Activity measurement method Dissolve ABTS in 25 mM citrate buffer (pH 3.2) at a concentration of 1.0 mg / ml to prepare a substrate solution. Take 3.0 ml of this substrate solution into a cuvette, preheat at 25 ° C., add 0.1 ml of enzyme solution, stir, incubate at 25 ° C., and measure the absorbance at 405 nm after 1 minute and 3 minutes. Under this condition, the amount of enzyme that increases the absorbance at 405 nm by 1.0 OD per minute is defined as 1 unit.
  • the enzyme activity of protein glutaminase was measured by the method described below using Z-Gln-Gly as a substrate unless otherwise specified.
  • ⁇ Activity measurement method> Add 10 ⁇ l of enzyme solution to 100 ⁇ l of 176 mmol / l phosphate buffer (pH 6.5) containing 10 mmol / l Z-Gln-Gly, incubate at 37 ° C for 60 minutes, and then add 100 ⁇ l of 12% trichloroacetic acid solution for reaction. To stop. After centrifugation (15000 rpm, 4 ° C., 5 minutes), the supernatant is measured using F-kitammonia (manufactured by Beringer Mannheim) as follows (A1).
  • reaction solution After completion of the reaction, a part of the reaction solution was separated and subjected to 2 to 25% polyacrylamide gel electrophoresis to observe an increase in the molecular weight of the substrate protein, and cross-linking and cross-linking based on the case where laccase was used alone. It was judged to be a promoting effect.
  • the amount of enzyme added was 100 U for laccase (final concentration) and 500 mU for protein glutaminase (final concentration) per 1 mg of substrate protein.
  • LYZAMINE-S pea protein, manufactured by Rocket Japan.
  • reaction solution After completion of the reaction, a part of the reaction solution was separated and subjected to 2 to 25% polyacrylamide gel electrophoresis to observe an increase in the molecular weight of the substrate protein, and cross-linking and cross-linking based on the case where laccase was used alone. It was judged to be a promoting effect.
  • the amount of enzyme added was 100 U for laccase (final concentration) and 500 mU for protein glutaminase (final concentration) per 1 mg of substrate protein.
  • the amount of enzyme added was 100 U for laccase (final concentration) and 500 mU for protein glutaminase (final concentration) per 1 mg of substrate protein.
  • the same reaction was carried out under the condition that both the amount of enzyme added (laccase and protein glutaminase) was reduced to 1/10 and 1/100.
  • the efficiency of cross-linking polymerization of the substrate protein is improved by the combined use of laccase and protein glutaminase as compared with the case of using laccase alone, and the polyacrylamide gel cannot pass through the network at any enzyme concentration.
  • the band of the polymerized protein (the band that can be confirmed at the top of each lane (lanes 5 to 7)) was confirmed to be darker, and cross-linked polymerization was observed. That is, the combined use of protein glutaminase with laccase was found to have an effect of promoting cross-linking of soybean-derived protein.
  • Example 4 The effect of promoting protein cross-linking by the combined use of laccase and protein glutaminase was examined by a method using egg-derived albumin (manufactured by Fujifilm Wako Pure Chemical Industries, Ltd.). Egg-derived albumin mixed with 5% by weight (final concentration) of 50 mM (final concentration) potassium / sodium phosphate buffer (pH 7.0) and protein glutaminase (product name: protein glutaminase "Amano" 500, manufactured by Amano Enzyme Co., Ltd.) After that, it was carried out at 40 ° C. for 4 hours with shaking at 160 rpm.
  • egg-derived albumin manufactured by Fujifilm Wako Pure Chemical Industries, Ltd.
  • Egg-derived albumin mixed with 5% by weight (final concentration) of 50 mM (final concentration) potassium / sodium phosphate buffer (pH 7.0) and protein glutaminase (product name: protein glutaminase "Amano" 500, manufactured by Amano Enzyme
  • laccase product name: laccase Y120, manufactured by Amano Enzyme Co., Ltd.
  • laccase product name: laccase Y120, manufactured by Amano Enzyme Co., Ltd.
  • the amount of enzyme added was 100 U for laccase (final concentration) and 500 mU for protein glutaminase (final concentration) per 1 mg of substrate protein.
  • the amount of enzyme added was 100 U for laccase (final concentration) and 500 mU for protein glutaminase (final concentration) per 1 mg of substrate protein.
  • the same reaction was also carried out under the condition that the amount of enzyme added (laccase and protein glutaminase) was diluted together.
  • the efficiency of cross-linking polymerization of the substrate protein is improved by the combined use of laccase and protein glutaminase as compared with the case of using laccase alone, and the protein polymerized to about 200 kDa or more at any enzyme concentration.
  • laccase 5-7 That is, the combined use of protein glutaminase with laccase was found to have an effect of promoting cross-linking of almond-derived proteins.
  • the amount of enzyme added was 100 U for laccase (final concentration) and 500 mU for protein glutaminase (final concentration) per 1 mg of substrate protein.
  • the same reaction was also carried out under the condition that the amount of enzyme added (laccase and protein glutaminase) was diluted together.
  • the efficiency of cross-linking polymerization of the substrate protein is improved by the combined use of laccase and protein glutaminase as compared with the case of using laccase alone, and it is impossible to pass through the network of polyacrylamide gel at any enzyme concentration.
  • the band of the polymerized protein (the band that can be confirmed at the top of each lane (lanes 5 to 7)) was confirmed to be darker, and cross-linked polymerization was observed. That is, the combined use of protein glutaminase with laccase was found to have an effect of promoting cross-linking of chickpea-derived protein.
  • the efficiency of cross-linking polymerization of the substrate protein is improved by the combined use of bilirubin oxidase and protein glutaminase as compared with the case of using bilirubin oxidase alone, and the band of the polymerized protein is improved at any enzyme concentration.
  • the band of the polymerized protein is improved at any enzyme concentration.
  • the amount of enzyme added was 100 U for tyrosinase (final concentration) and 500 mU for protein glutaminase (final concentration) per 1 mg of substrate protein.
  • the same reaction was carried out under the condition that the amount of enzyme added (tyrosinase and protein glutaminase) was diluted together.
  • the efficiency of cross-linking polymerization of the substrate protein is improved by the combined use of tyrosinase and protein glutaminase as compared with the case of using tyrosinase alone, and the polymerized protein bands are formed at any enzyme concentration. Darker confirmation was observed in the upper part of the lanes (lanes 5 to 6), and / or a newly confirmed band of polymerized protein was confirmed at the top of each lane (lanes 6 to 7), and crosslinked polymerization was observed. .. That is, the combined use of protein glutaminase with tyrosinase was found to have an effect of promoting cross-linking of casein protein.
  • the shear rate at the time of measurement was 200 s-1, and a preliminary measurement was performed for 30 seconds in order to maintain the flow state.
  • an enzyme-free casein solution, a laccase (50 U / mL) -treated casein solution and a protein glutaminase (100 mU / mL) -treated casein solution were also measured as controls.
  • the efficiency of cross-linking polymerization of the substrate protein was improved by the combined use of laccase and protein glutaminase as compared with the case of using laccase alone, and the polymer was polymerized to 200 kDa or more at any enzyme concentration. The presence of the protein was newly confirmed, and cross-linked polymerization was observed.
  • the crosslinked, polymerized, or gelled protein materials produced by the present invention include, for example, fish meat pastes, sardines, fish / livestock sausages, tofu, noodles, confectionery / bread making, food adhesives, and meat sheets. It is used in the food processing field such as ready-to-eat foods, yogurt, jelly, cheese, and substitute meat / dairy products (substitute cheese, alternative milk fermented food) made from plant materials.
  • novel protein-derived material it is expected to be used in a wide range of industries including cosmetics, medical products, materials for microcapsules, and carriers such as immobilized enzymes. Since the reaction mechanism of cross-linking by oxidoreductase is considered to be different from that of transglutaminase, which is frequently used for cross-linking proteins, it is possible to produce protein polymerized products and gel-like substances having new qualities. The use and application of the present invention can also be expected.

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Abstract

La présente invention aborde le problème de la fourniture d'un nouveau procédé de réticulation de protéines. Dans la présente invention, une réaction de réticulation est accélérée en amenant à la fois une oxydoréductase telle qu'une laccase et une protéine désamidase telle qu'une protéine glutaminase à agir sur une protéine de substrat.
PCT/JP2021/010764 2020-03-17 2021-03-17 Procédé de réticulation de protéines Ceased WO2021187510A1 (fr)

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JP2022508399A JPWO2021187510A1 (fr) 2020-03-17 2021-03-17
CA3171481A CA3171481A1 (fr) 2020-03-17 2021-03-17 Procede de reticulation de proteines
CN202180020879.4A CN115298320A (zh) 2020-03-17 2021-03-17 蛋白质的交联方法
BR112022017511A BR112022017511A2 (pt) 2020-03-17 2021-03-17 Método de reticulação de proteína
US17/906,498 US20230114377A1 (en) 2020-03-17 2021-03-17 Protein crosslinking method

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WO2022202889A1 (fr) * 2021-03-23 2022-09-29 天野エンザイム株式会社 Procédé de fabrication d'une boisson de soja traitée
CN115350329A (zh) * 2022-08-19 2022-11-18 江苏西宏生物医药有限公司 一种长效微粒ⅰ型与iii型胶原蛋白复合植入剂
WO2023048195A1 (fr) * 2021-09-21 2023-03-30 天野エンザイム株式会社 Procédé de production de boisson ou d'aliment fermenté à base de protéines
WO2023085315A1 (fr) * 2021-11-09 2023-05-19 天野エンザイム株式会社 Activateur de digestibilité pour composition contenant une protéine botanique
WO2023085316A1 (fr) * 2021-11-09 2023-05-19 天野エンザイム株式会社 Procédé de production d'un produit alimentaire contenant une protéine végétale texturée
WO2024171196A1 (fr) * 2023-02-15 2024-08-22 Enzymofit Ltd. Hydrogels de protéines végétales biodégradables, leurs utilisations et leur préparation

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CN115317668B (zh) * 2022-08-19 2023-12-29 北京西宏润美医药科技有限公司 一种长效微粒ⅰ型胶原蛋白植入剂
CN119318380A (zh) * 2024-10-18 2025-01-17 南京农业大学 一种基于复合酶处理用于猪头肉质构重组的方法

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Publication number Priority date Publication date Assignee Title
WO2022202889A1 (fr) * 2021-03-23 2022-09-29 天野エンザイム株式会社 Procédé de fabrication d'une boisson de soja traitée
WO2023048195A1 (fr) * 2021-09-21 2023-03-30 天野エンザイム株式会社 Procédé de production de boisson ou d'aliment fermenté à base de protéines
WO2023085315A1 (fr) * 2021-11-09 2023-05-19 天野エンザイム株式会社 Activateur de digestibilité pour composition contenant une protéine botanique
WO2023085316A1 (fr) * 2021-11-09 2023-05-19 天野エンザイム株式会社 Procédé de production d'un produit alimentaire contenant une protéine végétale texturée
CN115350329A (zh) * 2022-08-19 2022-11-18 江苏西宏生物医药有限公司 一种长效微粒ⅰ型与iii型胶原蛋白复合植入剂
WO2024171196A1 (fr) * 2023-02-15 2024-08-22 Enzymofit Ltd. Hydrogels de protéines végétales biodégradables, leurs utilisations et leur préparation

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